Detection of neurophysiological features in female R255X MeCP2 mutation mice

Rett syndrome (RTT) is a severe neurodevelopmental disorder (NDD) that is nearly always caused by loss of function mutations in Methyl-CpG-binding Protein 2 (MECP2) and shares many clinical features with other NDD. Genetic restoration of Mecp2 in symptomatic mice lacking MeCP2 expression can reverse...

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Detalles Bibliográficos
Autores principales: Dong, Hong-Wei, Erickson, Kirsty, Lee, Jessica R., Merritt, Jonathan, Fu, Cary, Neul, Jeffrey L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572861/
https://www.ncbi.nlm.nih.gov/pubmed/32927061
http://dx.doi.org/10.1016/j.nbd.2020.105083

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572861/
https://www.ncbi.nlm.nih.gov/pubmed/32927061
http://dx.doi.org/10.1016/j.nbd.2020.105083

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